SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs27903719 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65616681 | ACCCCAAATTATTTC[C/T]TGGTGGCAGTGTCTT | 69807 |
rs27903720 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65616633 | TAAGCCAAAGCTTTT[A/G]CTTTCCTCGAAACAA | 69807 |
rs27903721 | snp | C/T | 0.32 | 0.24 | downstream-variant-500B, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65616311 | TATTATGCCATTCTG[C/T]TTATCTATACTGTAT | 69807 |
rs27903722 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65616132 | AGAACAAACTGTTAG[A/G]TAGCTAGCTCTGTAT | 69807 |
rs27903723 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65616067 | GAATTGTGTAATGTG[A/G]GCTTCGACCAACAAT | 69807 |
rs27903724 | snp | C/T | 0.142012 | 0.225474 | utr-variant-3-prime, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65616034 | CCTTCCACTGACCTA[C/T]GCTAAGAGTTATTGA | 69807 |
rs27903725 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65615982 | AACATATCCAGCAAA[C/T]GTGGGATATTTTCTA | 69807 |
rs27903726 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65615696 | ATATTCTGTAGCATG[A/G]TGTCTCCTTTGATCA | 69807 |
rs27903727 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65615666 | GTGGGATCTGCTTGA[A/C]CCTTCAGTGATATTA | 69807 |
rs27903728 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65615593 | TACTGTCTCCTTCCT[G/T]TTACAGTGTGCTTCG | 69807 |
rs27903729 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65613684 | GACTCGTCTAAGGGA[A/G]CTTACTGGAGAGCTG | 69807 |
rs27903730 | snp | G/T | 0.32 | 0.24 | utr-variant-5-prime, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65613165 | TGAATATTAAGCTGT[G/T]TGGCTCTAAGCTGTG | 69807 |
rs27903731 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612808 | CGGCAGGGTTATTCT[C/G]TGCTTTCCTGCTTGT | 69807 |
rs27903732 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612680 | CGCCTCTAAGATTTG[C/T]AAGACTTCTCTTACA | 69807 |
rs27903733 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612599 | GCCATCAACTGTGAT[A/G]GAATGAAAAGGCTTG | 69807 |
rs27903734 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612537 | GATGGTTTGCAGGTT[A/G]CTTAAAGGCAATCAT | 69807 |
rs27903735 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612247 | GTGTTTCGTTCTCCC[A/G]TCTCATTTCTGTGCC | 69807 |
rs27903736 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612202 | TGCCATCTGCTTTCT[C/T]GGCTGTATTCAGGCT | 69807 |
rs27903737 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612150 | AGATAGACCAAGCGT[C/T]CCCTGTTCTTCGTCC | 69807 |
rs27903738 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612131 | TTTACAGATGCAGAA[A/T]TTTAGATAGACCAAG | 69807 |
rs27903739 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612114 | GGATATGCTGTCTCC[A/G]TTTTACAGATGCAGA | 69807 |
rs27903740 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65611975 | ATCCTCAAATGGTTA[C/G]ATCTCTGTGCATCTC | 69807 |
rs27903741 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65611915 | ACAAAGAATGTCCCA[C/T]GTTACTTGCACATGA | 69807 |
rs27903742 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65611459 | GTCCTAGAGCAGAGT[C/T]GAGAGCACTCTTTAA | 69807 |
rs27903743 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65611274 | AAGTTCATGCTGCCC[A/G]GTAATTTGTTGTTTT | 69807 |
rs27903744 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65611166 | GCAGATCTTGGGTCA[A/G]GGCTTCTATTGGTGT | 69807 |
rs27903745 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610869 | AAATAGTTTGCCATT[A/G]GATGTGGGCATAATC | 69807 |
rs27903746 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610816 | TGCATGGATTTTTGA[C/T]ATCTTTTTGGAGAAC | 69807 |
rs27903747 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610740 | ACTGGGATGGTGGTG[A/G]TAACAGAAATAAGTC | 69807 |
rs27903748 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610696 | CTGCCAGACTGGTGG[A/G]TCTGTCTTAGGCTAA | 69807 |
rs27903749 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610554 | CATCTGAAGGCTTGG[C/T]ATAGGGAGGCAGTTC | 69807 |
rs27903750 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610464 | GTGGAGGCAGCCAAG[A/G]TTGTAAATGGCGTGT | 69807 |
rs27903751 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610146 | CTTGTTCTGTCTCCC[G/T]TCAAGGTTTATGTTA | 69807 |
rs27903752 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65609898 | TAGTTCTCATGGTAA[A/T]TTTCTCTCTCTCTCT | 69807 |
rs27903753 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65609479 | TCCAGGAGAGGACAA[A/T]TCTTCATTCCTTTCA | 69807 |
rs27903754 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65609069 | ATCACCTTGAAAGGC[C/T]ATTTCATACCTAAGT | 69807 |
rs27903755 | snp | A/C | 0.32 | 0.24 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608727 | ATTGCTTAAGGTTCG[A/C]CAGGTTTGCTTATGG | 69807 |
rs27903756 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608662 | CCATCTCCATCCATC[A/G]TGGCAGGACTACACT | 69807 |
rs27903757 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608472 | ACTTGGTTCGAATTG[A/G]GTTAAAGTGCATAAG | 69807 |
rs27903758 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608348 | TTTAGCTATCAGCAG[C/G]CACCATAAGTGCCCT | 69807 |
rs27903759 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608301 | AGGGTTCCTGGCACT[C/T]GTTACTCCAGATGGC | 69807 |
rs27903760 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608252 | TGGACTAACACTTCC[G/T]TCACACAGTTAAGAG | 69807 |
rs27903761 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608139 | GGTGAGCCCTTTTGT[A/G]GCCCAGTTCACAGAT | 69807 |
rs27903762 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607797 | AGCCTCCTAGAGTGC[A/G]CCCTCCTGTATGCAG | 69807 |
rs27903763 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607728 | AATGACATATCCTGG[C/G]TTACAGAGCAAGTGG | 69807 |
rs27903764 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607708 | AAGTGAAGAGCCACT[A/T]GTTAAATGACATATC | 69807 |
rs27903765 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607679 | AAATGTTACTCCTGA[C/T]TCTACAAGGCAGAAA | 69807 |
rs27903766 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607639 | TGCTGATTAATGTGC[A/G]TTCTCTCCATAAGGC | 69807 |
rs27903767 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607631 | CGGCTGAGTGCTGAT[C/T]AATGTGCATTCTCTC | 69807 |
rs27918768 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607569 | TGTTTTACTGCTTGC[G/T]TGGTGGTCAAGCACT | 69807 |
rs27918769 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607516 | TCAGATCGCTTAGGA[A/G]AACACCTGACGGAGG | 69807 |
rs27918770 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607489 | AGAACACTTAGCTGC[C/G]ATGACATCAACTCAG | 69807 |
rs27918771 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607177 | GGAAAGGGAGGCTTG[C/T]CCCGTAGTCAGAAGC | 69807 |
rs27918772 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65606047 | GCATAACTGAACCCA[G/T]AGGGTCTTCTGGAGA | 69807 |
rs27918773 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65605940 | GGTGGGGAGTGAATG[C/T]TGTAACTAGATTATA | 69807 |
rs27918774 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65605781 | GATAGATGTGGGAAT[C/T]TGAAAATAGATTAAA | 69807 |
rs27918775 | snp | A/C | 0.32 | 0.24 | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65605590 | TCAGTACCCAGTTAG[A/C]AAATCGCAGCAAAGG | 69807 |
rs27918776 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime | Trim32, Astn2 | Mm_Celera | 4:65605356 | GACGTCCCTGGAGGT[A/G]TCTGGGTGCAGAATA | 69807 |
rs27918777 | snp | C/T | 0.124444 | 0.216185 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Trim32, Astn2 | Mm_Celera | 4:65605165 | ACTGGATCGGAGTGG[C/T]AGGATCGGATTCGGA | 69807 |
rs27918778 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65604872 | TCCGGAGCCATCCCT[A/G]TCTATTCAGCTGGGC | 69807 |
rs27918779 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65604552 | GCCACAAAACCTCCC[A/G]TCTGACAAGGCTCAA | 69807 |
rs27918780 | snp | G/T | 0.124444 | 0.216185 | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65604480 | TACTGTGTGTTTATC[G/T]CATTCAGGAGCAGGT | 69807 |
rs27918781 | snp | A/T | 0.231111 | 0.249285 | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65604403 | GTGCAGAGGGTACAC[A/T]GCTAGGTGGAATTTC | 69807 |
rs27918782 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65604318 | CTAGGTCTCAGCTTC[C/T]TTTCAAAGTCTGTAG | 69807 |
rs27918783 | snp | C/G | 0.336735 | 0.234472 | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65604273 | GCCAGGTTCTGACAG[C/G]TAGAAACTGGTTACT | 69807 |
rs27918784 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65603886 | CATATTCTCTGGGAA[A/G]GCCTTGGGAGTTCTG | 69807 |
rs27918785 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65603318 | TAATGCAACCTGTTA[C/T]GAAGTGAGTTCCACA | 69807 |
rs50850970 | snp | A/G | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65609663 | CCTGGAACTCACTCT[A/G]TAGACCAGGCTGGCC | 69807 |
rs52519898 | snp | G/T | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65609633 | GACAGGGTTTCTCTG[G/T]GTATCCCTGGCTGTC | 69807 |
rs108639438 | snp | G/T | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65609575 | TGGTTTTTGTTTTGG[G/T]TTTTTTTTTTTTTTT | 69807 |
rs211762436 | snp | A/G | | | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65603710 | GATTGTTAGGCCAGA[A/G]TCATAGGTTGTTAAT | 69807 |
rs211778744 | snp | A/G | | | synonymous-codon, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65613984 | CCTGGAGGAGACAGC[A/G]GATGAGGAGGAGCCC | 69807 |
rs211814024 | snp | A/G | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612679 | TCGCCTCTAAGATTT[A/G]TAAGACTTCTCTTAC | 69807 |
rs213142808 | snp | A/G | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610118 | TCTGTAAGTGAAGGC[A/G]CAACAATGCTGTCTT | 69807 |
rs213438536 | snp | A/G | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65605854 | AATTGCAAGGCTGCA[A/G]CATACAGTCTAAAAG | 69807 |
rs213867220 | snp | A/C | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607912 | CAACCTCTAAGCCAA[A/C]TCTTACCTGCAGGTA | 69807 |
rs214327567 | snp | A/T | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607501 | TGCGATGACATCAAC[A/T]CAGATCGCTTAGGAA | 69807 |
rs214431682 | snp | A/T | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65611716 | TAGGATACCAGAGCA[A/T]TTTTCTGCCTATAGA | 69807 |
rs215106937 | snp | A/G | | | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65603696 | CCTTATAGTCAGAAG[A/G]TTGTTAGGCCAGAGT | 69807 |
rs215123456 | snp | C/T | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607197 | TAGTCAGAAGCTGGG[C/T]GACTTCTCTTGATTA | 69807 |
rs215159131 | snp | C/T | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65606493 | GGAGCCTCCTGTCTA[C/T]TGAGTATTTAGCCTG | 69807 |
rs215648466 | snp | G/T | | | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65604465 | CATATTCCTCACTAG[G/T]ACTGTGTGTTTATCG | 69807 |
rs215683794 | snp | A/C | | | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65604009 | ATGTGAGAACTCCTG[A/C]ATCACTGAGAAGAGA | 69807 |
rs215717057 | snp | C/T | | | synonymous-codon, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65614809 | CTACTTCACCCAAGG[C/T]TTGGGGCTCAATGTG | 69807 |
rs215938303 | snp | G/T | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608846 | TTATTTCAATGTATG[G/T]CTGCTGCCTTAGGCA | 69807 |
rs216344291 | snp | G/T | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65609754 | GAGCCACGACTGCCC[G/T]GCTCTGGTTCTGATT | 69807 |
rs216376726 | snp | A/T | | | downstream-variant-500B, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65616516 | AAATGAAGACAGCTA[A/T]GTATATGTGTTTCAG | 69807 |
rs216988531 | snp | A/G | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65611460 | TCCTAGAGCAGAGTC[A/G]AGAGCACTCTTTAAT | 69807 |
rs217019994 | snp | A/C | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610215 | ATTTCACAGACTGGA[A/C]AAATTCAGTGGTGTC | 69807 |
rs217291301 | snp | A/G | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65607111 | CACATCCTCTCTTCC[A/G]TTGCTGGTTTGCTGC | 69807 |
rs217324468 | snp | A/C | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65606277 | CACTCTGACCACCCC[A/C]ACCTCCTCATCACAG | 69807 |
rs217394343 | snp | C/G | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608704 | CTTAGGAAAGATCTG[C/G]TTCGTTAATTGCTTA | 69807 |
rs217394889 | snp | A/G | | | downstream-variant-500B, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65616690 | TATTTCTTGGTGGCA[A/G]TGTCTTTATAGCTGT | 69807 |
rs217418958 | snp | A/G | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65608057 | GCCTCCCAAGTGCTG[A/G]GATTCAAGGCGTGAG | 69807 |
rs217893512 | snp | G/T | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65610835 | TTTTTGGAGAACCTG[G/T]TAAAACTGTAGACTG | 69807 |
rs218094578 | in-del | -/C | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65605650 | GGCGGAGGTGGGGGG[-/C]GGGGGTTGGAGGTGG | 69807 |
rs218297055 | snp | A/T | | | intron-variant | Trim32, Astn2 | Mm_Celera | 4:65612906 | TCCATAACATAATGC[A/T]TTAATCATTTGTGTG | 69807 |
rs218549737 | in-del | -/TGCCCGAGTTC | | | intron-variant | Trim32, Astn2 | GRCm38.p3 | 4:65609213 | CAACCCATGCCCCTT[-/TGCCCGAGTTC]TGCCTTAGGATGTGG | 69807 |
rs219188189 | in-del | -/TCCCCC | | | cds-indel, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65615350 | TTGTTATGCCCCTCT[-/TCCCCC]CCCCCCTCCCCTTTT | 69807 |
rs219216657 | in-del | -/C | | | upstream-variant-2KB, intron-variant | Trim32, Astn2 | Mm_Celera | 4:65604246 | GTTAAGAGTGATTCT[-/C]GGGAAATTAAAGCCA | 69807 |